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Research 481–510 of 1000+
- Continuous MEK inhibition by AZD6244 (ARRY-142886) results in exhaustion of the cutaneous keratinocytic stem cell pool and resembles senescence driven skin aging
- Alopecia areata: current concepts
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Advanced Medical Therapies in the Management of Non-Scarring Alopecia: Areata and Androgenic Alopecia
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- JAAD Grand Rounds quiz∗
- Alopecia in Rhesus macaques correlates with immunophenotypic alterations in dermal inflammatory infiltrates consistent with hypersensitivity etiology
- Development and homeostasis of the sebaceous gland
- Double mutation of <i>claudin‐1</i> and <i>claudin‐3</i> causes alopecia in infant mice
- Viewpoint 4
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Telogen effluvium and associated incidence of abnormal serum ferritin, zinc, 25-hydroxy vitamin D, and thyroid-stimulating hormone
- Congenital hypotrichosis due to short anagen
- Hormone und Haarwachstum
- Short anagen syndrome in an African American woman
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- CD44 signaling in skin wound healing and regeneration
- Myeloproliferative disorder associated with alopecia universalis
- Short Anagen Syndrome in an Indian Woman with its Impact on Quality-of-Life
- Circle hairs involving the extremities in a young girl
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Hypotrichosis with juvenile macular dystrophy
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- IgG/IgA pemphigus with differing regional presentations